Page last updated: 2024-10-21

7-nitroindazole and HIV

7-nitroindazole has been researched along with HIV in 1 studies

7-nitroindazole: an inhibitor of nitric oxide synthase; exhibits anti-nociceptive activity without increasing blood pressure

HIV: Human immunodeficiency virus. A non-taxonomic and historical term referring to any of two species, specifically HIV-1 and/or HIV-2. Prior to 1986, this was called human T-lymphotropic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV). From 1986-1990, it was an official species called HIV. Since 1991, HIV was no longer considered an official species name; the two species were designated HIV-1 and HIV-2.

Research Excerpts

ExcerptRelevanceReference
"New 2-bromomethyl-8-substituted-benzo[c]chromen-6-ones have been synthesized and their bioactive properties have been evaluated on different enzymatic models: serine proteases (trypsin and alpha-chymotrypsin), HIV aspartyl protease, nitric oxide synthase and a panel of protein kinases."3.73New 2-bromomethyl-8-substituted-benzo[c]chromen-6-ones. Synthesis and biological properties. ( Bain, J; Bihel, F; Boucher, JL; Garino, C; Klein, P; Kraus, JL; Laras, Y; Pietrancosta, N; Quéléver, G; Woo, I, 2005)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Garino, C1
Bihel, F1
Pietrancosta, N1
Laras, Y1
Quéléver, G1
Woo, I1
Klein, P1
Bain, J1
Boucher, JL1
Kraus, JL1

Other Studies

1 other study available for 7-nitroindazole and HIV

ArticleYear
New 2-bromomethyl-8-substituted-benzo[c]chromen-6-ones. Synthesis and biological properties.
    Bioorganic & medicinal chemistry letters, 2005, Jan-03, Volume: 15, Issue:1

    Topics: Aspartic Acid Endopeptidases; Benzopyrans; Chymotrypsin; HIV; Molecular Structure; Nitric Oxide Synt

2005